| Dataset | OMIM Gene-Disease Associations |
| Category | disease or phenotype associations |
| Type | phenotype |
| External Link | http://www.omim.org/entry/113750 |
| Similar Terms | |
| Downloads & Tools |
1 genes associated with the albinism, oculocutaneous, type vi phenotype from the curated OMIM Gene-Disease Associations dataset.
| Symbol | Name |
|---|---|
| SLC24A5 | solute carrier family 24 (sodium/potassium/calcium exchanger), member 5 |
